ALOKA UST-5514DTU-7.5 LINEAR DOPPLER TRANSDUCER— 510(k) K901335

Name: FDA 510(k) clearance K901335
Creator: U.S. Food and Drug Administration
Published: 1990-08-10

Substantially Equivalent

Ge Medical Systems Information Technologies

FDA 510(k) clearance K901335 for ALOKA UST-5514DTU-7.5 LINEAR DOPPLER TRANSDUCER, Substantially Equivalent on 1990-08-10. Applicant: Ge Medical Systems Information Technologies. Device class: 2.

Clearance details

Applicant: Ge Medical Systems Information Technologies
Product code: Code DPW
Device class: Class 2
Regulation: 21 CFR 870.2100
Advisory panel: Cardiovascular
Date received: 1990-03-22
Decision date: 1990-08-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wallingford, CT, US

Download summary PDF View on FDA.gov ↗

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